A Dose Escalation and Dose Expansion Trial of WTX212A in the Treatment of Patients with Advanced Malignant Tumors
- Conditions
- Unresectable or Metastatic Advanced Solid Tumors
- Interventions
- Registration Number
- NCT06026605
- Lead Sponsor
- Zhejiang University
- Brief Summary
This trial is a multi-center, open-label investigator-initiated clinical study (IIT) to evaluate the safety, pharmacokinetics, pharmacodynamics and effectiveness of WTX212A injection in the treatment of patients with unresectable or metastatic advanced solid tumors who failed in previous systematic therapy.
The study was divided into two phases: dose escalation and dose expansion
- Detailed Description
The study was divided into two phases: dose escalation and dose expansion Detailed Description: This trial is a multi-center, open-label investigator-initiated clinical study(llT)to evaluate the safety, pharmacokinetics, pharmacodynamics and effectiveness of WTX212A injection in the treatment of patients with unresectable or metastatic advanced solid tumors who failed in previous systematic therapy.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 44
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- Must signs an informed consent form, understands this study, is willing to follow and has the ability to complete all experimental procedures; 2. Aged 18 to 75 years old (including threshold); 3. Histopathology diagnosed unresectable or metastatic solid tumors who have failed systemic treatment or have no effective standard treatment, or who are unwilling to accept standard treatment or are not suitable for standard treatment; 4. ECOG≤1； 5. Expected life ≥ 3 months； 6. Male participants, their spouses, and female participants of childbearing age should agree to use a medically recognized effective contraceptive method from the signing of the informed consent form until 3 months after the last administration; 7. Women of childbearing age must have a negative pregnancy testing results within ≤ 7 days before the first trial drug administration.
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- Other serious medical diseases, including but not limited to: uncontrolled diabetes, active peptic ulcer, active bleeding, etc., and people with uncontrollable or serious cardiovascular diseases, 2. Pleural and ascitic fluids with clinical symptoms and the need for repeated drainage; 3. Previous or recent history of pulmonary fibrosis, severe lung function damage caused by pneumoconiosis, radiation pneumonia, and drug-related pneumonia; 4. History of adverse events related to the use of IO drugs that require permanent cessation of IO treatment; 5. Known to have other malignant tumors, currently progressing or completing treatment at least once in the past 3 years.
- Symptomatic central nervous system (CNS) metastasis confirmed by imaging or pathological examination and clinically unstable for at least 14 days prior to enrollment who require steroid treatment; 7. Hereditary bleeding tendencies or coagulation disorders, or a history of thrombosis, hemolysis, or hemorrhagic diseases; 8. Received significant surgical treatment or obvious traumatic injury within 28 days prior to the start of research treatment;
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description WTX212A WTX212A WTX212A infusion once every 21 days
- Primary Outcome Measures
Name Time Method incidence of severe adverse events (SAE) through study completion, an average of 1 year The incidence of SAE during the treatment of WTX212A injection
incidence of adverse events through study completion, an average of 1 year The incidence of Adverse Events during the treatment of WTX212A injection
incidence of treatment related adverse events (TRAE) through study completion, an average of 1 year The incidence of TRAE during the treatment of WTX212A injection
- Secondary Outcome Measures
Name Time Method Cmin,ss through study completion, an average of 1 months Cmin,ss
Cmax,ss through study completion, an average of 1 months Cmax,ss
AUC（0-τ）ss. through study completion, an average of 1 months AUC（0-τ）ss.
Tmax through study completion, an average of 1 months Tmax
AUC0-t through study completion, an average of 1 months AUC0-t
Tmax,ss through study completion, an average of 1 months Tmax,ss
the occupancy rate of PD-1 receptor on the surface of peripheral blood T cells through study completion, an average of 1 year the occupancy rate of PD-1 receptor on the surface of peripheral blood T cells in subjects after WTX212A infusion
Cmax through study completion, an average of 1 months Cmax
t1/2 through study completion, an average of 1 months t1/2
CL through study completion, an average of 1 months CL
Objecive Response Rate (ORR) through study completion, an average of 4 months According to Response Evaluation Criteria In Solid Tumors Version 1.1
Anti-drug antibody (ADA) through study completion, an average of 1 year escribe the number and percentage of anti-drug antibodies (ADA) produced by subjects at each time point after treatment, and the time of producing ADA
Trial Locations
- Locations (1)
the First Affiliated Hospital, School of Medicine, Zhejiang University
🇨🇳Hangzhou, Zhejiang, China